| Year |
Citation |
Score |
| 2023 |
Heng E, Thanedar S, Heng HH. Challenges and Opportunities for Clinical Cytogenetics in the 21st Century. Genes. 14. PMID 36833419 DOI: 10.3390/genes14020493 |
0.377 |
|
| 2021 |
Heng J, Heng HH. Genome Chaos, Information Creation, and Cancer Emergence: Searching for New Frameworks on the 50th Anniversary of the "War on Cancer". Genes. 13. PMID 35052441 DOI: 10.3390/genes13010101 |
0.308 |
|
| 2021 |
Heng J, Heng HH. Two-phased evolution: Genome chaos-mediated information creation and maintenance. Progress in Biophysics and Molecular Biology. PMID 33992670 DOI: 10.1016/j.pbiomolbio.2021.04.003 |
0.377 |
|
| 2020 |
Heng J, Heng HH. Genome chaos: Creating new genomic information essential for cancer macroevolution. Seminars in Cancer Biology. PMID 33189848 DOI: 10.1016/j.semcancer.2020.11.003 |
0.367 |
|
| 2020 |
Ye CJ, Sharpe Z, Heng HH. Origins and Consequences of Chromosomal Instability: From Cellular Adaptation to Genome Chaos-Mediated System Survival. Genes. 11. PMID 33008067 DOI: 10.3390/genes11101162 |
0.441 |
|
| 2020 |
Ye CJ, Chen J, Liu G, Heng HH. Somatic Genomic Mosaicism in Multiple Myeloma. Frontiers in Genetics. 11: 388. PMID 32391059 DOI: 10.3389/Fgene.2020.00388 |
0.387 |
|
| 2019 |
Ye CJ, Stilgenbauer L, Moy A, Liu G, Heng HH. What Is Karyotype Coding and Why Is Genomic Topology Important for Cancer and Evolution? Frontiers in Genetics. 10: 1082. PMID 31737054 DOI: 10.3389/Fgene.2019.01082 |
0.506 |
|
| 2019 |
Ye CJ, Sharpe Z, Alemara S, Mackenzie S, Liu G, Abdallah B, Horne S, Regan S, Heng HH. Micronuclei and Genome Chaos: Changing the System Inheritance. Genes. 10. PMID 31086101 DOI: 10.3390/Genes10050366 |
0.452 |
|
| 2018 |
Ye CJ, Regan S, Liu G, Alemara S, Heng HH. Understanding aneuploidy in cancer through the lens of system inheritance, fuzzy inheritance and emergence of new genome systems. Molecular Cytogenetics. 11: 31. PMID 29760781 DOI: 10.1186/S13039-018-0376-2 |
0.446 |
|
| 2018 |
Liu G, Ye CJ, Chowdhury SK, Abdallah BY, Horne SD, Nichols D, Heng HH. Detecting Chromosome Condensation Defects in Gulf War Illness Patients. Current Genomics. 19: 200-206. PMID 29606907 DOI: 10.2174/1389202918666170705150819 |
0.318 |
|
| 2018 |
Ye CJ, Liu G, Heng HH. Experimental Induction of Genome Chaos. Methods in Molecular Biology (Clifton, N.J.). 1769: 337-352. PMID 29564834 DOI: 10.1007/978-1-4939-7780-2_21 |
0.426 |
|
| 2017 |
Stepanenko AA, Heng HH. Transient and stable vector transfection: Pitfalls, off-target effects, artifacts. Mutation Research. 773: 91-103. PMID 28927539 DOI: 10.1016/J.Mrrev.2017.05.002 |
0.416 |
|
| 2017 |
Ye CJ, Heng HH. High Resolution Fiber-Fluorescence In Situ Hybridization. Methods in Molecular Biology (Clifton, N.J.). 1541: 151-166. PMID 27910022 DOI: 10.1007/978-1-4939-6703-2_14 |
0.306 |
|
| 2017 |
Horne SD, Wexler M, Stevens JB, Heng HH. Insights on processes of evolutionary tumor growth Atlas of Genetics and Cytogenetics in Oncology and Haematology. DOI: 10.4267/2042/62674 |
0.493 |
|
| 2016 |
Heng HH, Regan SM, Liu G, Ye CJ. Why it is crucial to analyze non clonal chromosome aberrations or NCCAs? Molecular Cytogenetics. 9: 15. PMID 26877768 DOI: 10.1186/s13039-016-0223-2 |
0.399 |
|
| 2014 |
Heng HH. Distinguishing constitutional and acquired nonclonal aneuploidy. Proceedings of the National Academy of Sciences of the United States of America. 111: E972. PMID 24488973 DOI: 10.1073/Pnas.1323636111 |
0.444 |
|
| 2014 |
Liu G, Stevens JB, Horne SD, Abdallah BY, Ye KJ, Bremer SW, Ye CJ, Chen DJ, Heng HH. Genome chaos: survival strategy during crisis. Cell Cycle (Georgetown, Tex.). 13: 528-37. PMID 24299711 DOI: 10.4161/Cc.27378 |
0.64 |
|
| 2014 |
Abdallah BY, Horne SD, Kurkinen M, Stevens JB, Liu G, Ye CJ, Barbat J, Bremer SW, Heng HH. Ovarian cancer evolution through stochastic genome alterations: defining the genomic role in ovarian cancer. Systems Biology in Reproductive Medicine. 60: 2-13. PMID 24147962 DOI: 10.3109/19396368.2013.837989 |
0.589 |
|
| 2014 |
Stevens JB, Liu G, Abdallah BY, Horne SD, Ye KJ, Bremer SW, Ye CJ, Krawetz SA, Heng HH. Unstable genomes elevate transcriptome dynamics. International Journal of Cancer. Journal International Du Cancer. 134: 2074-87. PMID 24122714 DOI: 10.1002/Ijc.28531 |
0.644 |
|
| 2014 |
Abdallah B, Stevens JB, Horne S, Liu G, Heng HH. Abstract 2413: Unstable genomes and the average cancer cell Cancer Research. 74: 2413-2413. DOI: 10.1158/1538-7445.Am2014-2413 |
0.609 |
|
| 2013 |
Abdallah BY, Horne SD, Stevens JB, Liu G, Ying AY, Vanderhyden B, Krawetz SA, Gorelick R, Heng HH. Single cell heterogeneity: why unstable genomes are incompatible with average profiles. Cell Cycle (Georgetown, Tex.). 12: 3640-9. PMID 24091732 DOI: 10.4161/Cc.26580 |
0.549 |
|
| 2013 |
Heng HH. Genomics: HeLa genome versus donor's genome. Nature. 501: 167. PMID 24025829 DOI: 10.1038/501167D |
0.362 |
|
| 2013 |
Heng HH, Bremer SW, Stevens JB, Horne SD, Liu G, Abdallah BY, Ye KJ, Ye CJ. Chromosomal instability (CIN): what it is and why it is crucial to cancer evolution. Cancer Metastasis Reviews. 32: 325-40. PMID 23605440 DOI: 10.1007/S10555-013-9427-7 |
0.664 |
|
| 2013 |
Heng HH. Special issue: Genome instability and cancer. Preface. Cancer Metastasis Reviews. 32: 323-4. PMID 23595308 DOI: 10.1007/S10555-013-9432-X |
0.408 |
|
| 2013 |
Stevens JB, Horne SD, Abdallah BY, Ye CJ, Heng HH. Chromosomal instability and transcriptome dynamics in cancer. Cancer Metastasis Reviews. 32: 391-402. PMID 23595307 DOI: 10.1007/S10555-013-9428-6 |
0.655 |
|
| 2013 |
Heng HH, Liu G, Stevens JB, Abdallah BY, Horne SD, Ye KJ, Bremer SW, Chowdhury SK, Ye CJ. Karyotype heterogeneity and unclassified chromosomal abnormalities. Cytogenetic and Genome Research. 139: 144-57. PMID 23571381 DOI: 10.1159/000348682 |
0.648 |
|
| 2013 |
Stevens JB, Abdallah BY, Liu G, Horne SD, Bremer SW, Ye KJ, Huang JY, Kurkinen M, Ye CJ, Heng HH. Heterogeneity of cell death. Cytogenetic and Genome Research. 139: 164-73. PMID 23548436 DOI: 10.1159/000348679 |
0.479 |
|
| 2013 |
Horne SD, Abdallah BY, Stevens JB, Liu G, Ye KJ, Bremer SW, Heng HH. Genome constraint through sexual reproduction: application of 4D-Genomics in reproductive biology. Systems Biology in Reproductive Medicine. 59: 124-30. PMID 23294443 DOI: 10.3109/19396368.2012.754969 |
0.545 |
|
| 2013 |
Horne SD, Stevens JB, Abdallah BY, Liu G, Bremer SW, Ye CJ, Heng HH. Why imatinib remains an exception of cancer research. Journal of Cellular Physiology. 228: 665-70. PMID 23018746 DOI: 10.1002/Jcp.24233 |
0.532 |
|
| 2011 |
Heng HH, Stevens JB, Bremer SW, Liu G, Abdallah BY, Ye CJ. Evolutionary mechanisms and diversity in cancer. Advances in Cancer Research. 112: 217-53. PMID 21925306 DOI: 10.1016/B978-0-12-387688-1.00008-9 |
0.579 |
|
| 2011 |
Stevens JB, Abdallah BY, Liu G, Ye CJ, Horne SD, Wang G, Savasan S, Shekhar M, Krawetz SA, Hüttemann M, Tainsky MA, Wu GS, Xie Y, Zhang K, Heng HH. Diverse system stresses: common mechanisms of chromosome fragmentation. Cell Death & Disease. 2: e178. PMID 21716293 DOI: 10.1038/Cddis.2011.60 |
0.531 |
|
| 2011 |
Heng HH, Liu G, Stevens JB, Bremer SW, Ye KJ, Abdallah BY, Horne SD, Ye CJ. Decoding the genome beyond sequencing: the new phase of genomic research. Genomics. 98: 242-52. PMID 21640814 DOI: 10.1016/J.Ygeno.2011.05.008 |
0.58 |
|
| 2011 |
Johnson GD, Platts AE, Lalancette C, Goodrich R, Heng HH, Krawetz SA. Interrogating the transgenic genome: development of an interspecies tiling array. Systems Biology in Reproductive Medicine. 57: 54-62. PMID 21214491 DOI: 10.3109/19396368.2010.506000 |
0.362 |
|
| 2010 |
Stevens JB, Abdallah BY, Regan SM, Liu G, Bremer SW, Ye CJ, Heng HH. Comparison of mitotic cell death by chromosome fragmentation to premature chromosome condensation. Molecular Cytogenetics. 3: 20. PMID 20959006 DOI: 10.1186/1755-8166-3-20 |
0.658 |
|
| 2010 |
Heng HH, Liu G, Stevens JB, Bremer SW, Ye KJ, Ye CJ. Genetic and epigenetic heterogeneity in cancer: the ultimate challenge for drug therapy. Current Drug Targets. 11: 1304-16. PMID 20840073 DOI: 10.2174/1389450111007011304 |
0.582 |
|
| 2010 |
Heng HH, Stevens JB, Bremer SW, Ye KJ, Liu G, Ye CJ. The evolutionary mechanism of cancer. Journal of Cellular Biochemistry. 109: 1072-84. PMID 20213744 DOI: 10.1002/Jcb.22497 |
0.565 |
|
| 2009 |
Heng HH, Bremer SW, Stevens JB, Ye KJ, Liu G, Ye CJ. Genetic and epigenetic heterogeneity in cancer: a genome-centric perspective. Journal of Cellular Physiology. 220: 538-47. PMID 19441078 DOI: 10.1002/Jcp.21799 |
0.575 |
|
| 2009 |
Ye CJ, Stevens JB, Liu G, Bremer SW, Jaiswal AS, Ye KJ, Lin MF, Lawrenson L, Lancaster WD, Kurkinen M, Liao JD, Gairola CG, Shekhar MP, Narayan S, Miller FR, ... Heng HH, et al. Genome based cell population heterogeneity promotes tumorigenicity: the evolutionary mechanism of cancer. Journal of Cellular Physiology. 219: 288-300. PMID 19115235 DOI: 10.1002/Jcp.21663 |
0.596 |
|
| 2008 |
Heng HH, Stevens JB, Lawrenson L, Liu G, Ye KJ, Bremer SW, Ye CJ. Patterns of genome dynamics and cancer evolution. Cellular Oncology : the Official Journal of the International Society For Cellular Oncology. 30: 513-4. PMID 18936532 DOI: 10.3233/Clo-2008-0456 |
0.555 |
|
| 2007 |
Ye CJ, Liu G, Bremer SW, Heng HH. The dynamics of cancer chromosomes and genomes. Cytogenetic and Genome Research. 118: 237-46. PMID 18000376 DOI: 10.1159/000108306 |
0.428 |
|
| 2007 |
Stevens JB, Liu G, Bremer SW, Ye KJ, Xu W, Xu J, Sun Y, Wu GS, Savasan S, Krawetz SA, Ye CJ, Heng HH. Mitotic cell death by chromosome fragmentation. Cancer Research. 67: 7686-94. PMID 17699772 DOI: 10.1158/0008-5472.Can-07-0472 |
0.63 |
|
| 2006 |
DiPierdomenico J, Ying H, Lin F, Heng HH. A mathematical model relating chromosome aberrations to cancer progression. Conference Proceedings : ... Annual International Conference of the Ieee Engineering in Medicine and Biology Society. Ieee Engineering in Medicine and Biology Society. Annual Conference. 1: 2028-31. PMID 17946086 DOI: 10.1109/IEMBS.2006.260468 |
0.329 |
|
| 2006 |
Ye CJ, Stevens JB, Liu G, Ye KJ, Yang F, Bremer SW, Heng HH. Combined multicolor-FISH and immunostaining. Cytogenetic and Genome Research. 114: 227-34. PMID 16954658 DOI: 10.1159/000094205 |
0.56 |
|
| 2006 |
Heng HH, Stevens JB, Liu G, Bremer SW, Ye KJ, Reddy PV, Wu GS, Wang YA, Tainsky MA, Ye CJ. Stochastic cancer progression driven by non-clonal chromosome aberrations. Journal of Cellular Physiology. 208: 461-72. PMID 16688757 DOI: 10.1002/Jcp.20685 |
0.663 |
|
| 2006 |
Heng HH, Bremer SW, Stevens J, Ye KJ, Miller F, Liu G, Ye CJ. Cancer progression by non-clonal chromosome aberrations. Journal of Cellular Biochemistry. 98: 1424-35. PMID 16676347 DOI: 10.1002/Jcb.20964 |
0.618 |
|
| 2006 |
Heng HH, Liu G, Bremer S, Ye KJ, Stevens J, Ye CJ. Clonal and non-clonal chromosome aberrations and genome variation and aberration. Genome / National Research Council Canada = GéNome / Conseil National De Recherches Canada. 49: 195-204. PMID 16604101 DOI: 10.1139/G06-023 |
0.655 |
|
| 2005 |
Heng HH, Windle B, Tsui LC. High-resolution FISH analysis. Current Protocols in Human Genetics / Editorial Board, Jonathan L. Haines ... [Et Al.]. Unit 4.5. PMID 18428380 DOI: 10.1002/0471142905.hg0405s44 |
0.528 |
|
| 2005 |
Woodward KJ, Cundall M, Sperle K, Sistermans EA, Ross M, Howell G, Gribble SM, Burford DC, Carter NP, Hobson DL, Garbern JY, Kamholz J, Heng H, Hodes ME, Malcolm S, et al. Heterogeneous duplications in patients with Pelizaeus-Merzbacher disease suggest a mechanism of coupled homologous and nonhomologous recombination. American Journal of Human Genetics. 77: 966-87. PMID 16380909 DOI: 10.1086/498048 |
0.45 |
|
| 2005 |
Shen KC, Heng H, Wang Y, Lu S, Liu G, Deng CX, Brooks SC, Wang YA. ATM and p21 cooperate to suppress aneuploidy and subsequent tumor development. Cancer Research. 65: 8747-53. PMID 16204044 DOI: 10.1158/0008-5472.Can-05-1471 |
0.332 |
|
| 2004 |
Heng HH, Goetze S, Ye CJ, Liu G, Stevens JB, Bremer SW, Wykes SM, Bode J, Krawetz SA. Chromatin loops are selectively anchored using scaffold/matrix-attachment regions. Journal of Cell Science. 117: 999-1008. PMID 14996931 DOI: 10.1242/Jcs.00976 |
0.493 |
|
| 2004 |
Heng HH, Stevens JB, Liu G, Bremer SW, Ye CJ. Imaging genome abnormalities in cancer research. Cell & Chromosome. 3: 1. PMID 14720303 DOI: 10.1186/1475-9268-3-1 |
0.633 |
|
| 2003 |
Bode J, Goetze S, Heng H, Krawetz SA, Benham C. From DNA structure to gene expression: Mediators of nuclear compartmentalization and dynamics Chromosome Research. 11: 435-445. PMID 12971720 DOI: 10.1023/A:1024918525818 |
0.335 |
|
| 2003 |
Cheung J, Wilson MD, Zhang J, Khaja R, MacDonald JR, Heng HH, Koop BF, Scherer SW. Recent segmental and gene duplications in the mouse genome. Genome Biology. 4: R47. PMID 12914656 DOI: 10.1186/Gb-2003-4-8-R47 |
0.31 |
|
| 2003 |
Scherer SW, Cheung J, MacDonald JR, Osborne LR, Nakabayashi K, Herbrick JA, Carson AR, Parker-Katiraee L, Skaug J, Khaja R, Zhang J, Hudek AK, Li M, Haddad M, Duggan GE, ... ... Heng HH, et al. Human chromosome 7: DNA sequence and biology. Science (New York, N.Y.). 300: 767-72. PMID 12690205 DOI: 10.1126/Science.1083423 |
0.745 |
|
| 2001 |
Heng HH, Liu G, Lu W, Bremer S, Ye CJ, Hughes M, Moens P. Spectral karyotyping (SKY) of mouse meiotic chromosomes. Genome. 44: 293-8. PMID 11341740 DOI: 10.1139/g01-018 |
0.336 |
|
| 1999 |
Champagne N, Bertos NR, Pelletier N, Wang AH, Vezmar M, Yang Y, Heng HH, Yang XJ. Identification of a human histone acetyltransferase related to monocytic leukemia zinc finger protein. The Journal of Biological Chemistry. 274: 28528-36. PMID 10497217 DOI: 10.1074/Jbc.274.40.28528 |
0.314 |
|
| 1998 |
Motoyama J, Heng H, Crackower MA, Takabatake T, Takeshima K, Tsui LC, Hui CC. Overlapping and non-overlapping Ptch2 expression with Shh during mouse embryogenesis Mechanisms of Development. 78: 81-84. PMID 9858693 DOI: 10.1016/S0925-4773(98)00149-X |
0.557 |
|
| 1998 |
Crackower MA, Heng HH, Tsui LC. Assignment of mouse fibroblast growth factor 10 (Fgf10) gene to the telomeric region of chromosome 13. Genomics. 53: 247-8. PMID 9790778 DOI: 10.1006/Geno.1998.5506 |
0.583 |
|
| 1998 |
Pimenta AF, Tsui LC, Heng HH, Levitt P. Assignment of the gene encoding the limbic system-associated membrane protein (LAMP) to mouse chromosome 16B5 and human chromosome 3q13.2-q21. Genomics. 49: 472-4. PMID 9615236 DOI: 10.1006/Geno.1998.5280 |
0.596 |
|
| 1997 |
Crackower MA, Scherer SW, Heng HH, Tsui LC. Cloning of a DSS1 pseudogene (DSS1P1) and mapping to human Chromosome band 5ql4. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 8: 159-60. PMID 27518309 DOI: 10.1007/s003359900380 |
0.576 |
|
| 1997 |
Rozmahel R, Heng HH, Duncan AM, Shi XM, Rommens JM, Tsui LC. Amplification of CFTR exon 9 sequences to multiple locations in the human genome. Genomics. 45: 554-61. PMID 9367680 DOI: 10.1006/geno.1997.4968 |
0.329 |
|
| 1997 |
Osborne LR, Herbrick JA, Greavette T, Heng HH, Tsui LC, Scherer SW. PMS2-related genes flank the rearrangement breakpoints associated with Williams syndrome and other diseases on human chromosome 7. Genomics. 45: 402-6. PMID 9344666 DOI: 10.1006/Geno.1997.4923 |
0.62 |
|
| 1997 |
Okano K, Heng H, Trevisanato S, Tyers M, Varmuza S. Genomic organization and functional analysis of the murine protein phosphatase 1c gamma (Ppp1cc) gene. Genomics. 45: 211-5. PMID 9339378 DOI: 10.1006/Geno.1997.4907 |
0.428 |
|
| 1997 |
Crackower MA, Heng HH, Shi X, Scherer SW, Tsui LC. Fluorescent in situ mapping of the murine deleted in split hand/split foot 1 (dss1) gene to chromosome 6. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 8: 704. PMID 9271682 DOI: 10.1007/S003359900629 |
0.592 |
|
| 1997 |
Dong WF, Heng HH, Lowsky R, Xu Y, DeCoteau JF, Shi XM, Tsui LC, Minden MD. Cloning, expression, and chromosomal localization to 11p12-13 of a human LIM/HOMEOBOX gene, hLim-1. Dna and Cell Biology. 16: 671-8. PMID 9212161 DOI: 10.1089/Dna.1997.16.671 |
0.573 |
|
| 1997 |
Cohen D, Heng HH, Shi XM, McIntosh EM, Tsui LC, Pearlman RE. Assignment of the human dUTPase gene (DUT) to chromosome 15q15-q21. 1 by fluorescence in situ hybridization. Genomics. 40: 213-5. PMID 9070952 DOI: 10.1006/Geno.1996.4540 |
0.591 |
|
| 1997 |
Crackower MA, Scherer SW, Heng HH, Tsui LC. Cloning of a DSS1 pseudogene (DSS1P1) and mapping to human chromosome band 5q14. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 8: 159-60. PMID 9060422 |
0.304 |
|
| 1997 |
Tsukiyama-Kohara K, Vidal SM, Gingras AC, Glover TW, Hanash SM, Heng H, Sonenberg N. Tissue distribution, genomic structure, and chromosome mapping of mouse and human eukaryotic initiation factor 4E-binding proteins 1 and 2. Genomics. 38: 353-63. PMID 8975712 DOI: 10.1006/Geno.1996.0638 |
0.352 |
|
| 1996 |
Scherer SW, Duvoisin RM, Kuhn R, Heng HH, Belloni E, Tsui LC. Localization of two metabotropic glutamate receptor genes, GRM3 and GRM8, to human chromosome 7q. Genomics. 31: 230-3. PMID 8824806 DOI: 10.1006/Geno.1996.0036 |
0.34 |
|
| 1996 |
Osborne LR, Martindale D, Scherer SW, Shi XM, Huizenga J, Heng HH, Costa T, Pober B, Lew L, Brinkman J, Rommens J, Koop B, Tsui LC. Identification of genes from a 500-kb region at 7q11.23 that is commonly deleted in Williams syndrome patients. Genomics. 36: 328-36. PMID 8812460 DOI: 10.1006/Geno.1996.0469 |
0.609 |
|
| 1996 |
Kim KK, Youn BS, Heng HH, Shi XM, Tsui LC, Lee ZH, Pickard RT, Kwon BS. Genomic organization and FISH mapping of human Pmel 17, the putative silver locus. Pigment Cell Research. 9: 42-8. PMID 8739560 DOI: 10.1111/j.1600-0749.1996.tb00085.x |
0.396 |
|
| 1996 |
Wu HK, Heng HH, Siderovski DP, Dong WF, Okuno Y, Shi XM, Tsui LC, Minden MD. Identification of a human LIM-Hox gene, hLH-2, aberrantly expressed in chronic myelogenous leukaemia and located on 9q33-34.1. Oncogene. 12: 1205-12. PMID 8649822 |
0.329 |
|
| 1996 |
Heng HH, Chamberlain JW, Shi XM, Spyropoulos B, Tsui LC, Moens PB. Regulation of meiotic chromatin loop size by chromosomal position. Proceedings of the National Academy of Sciences of the United States of America. 93: 2795-800. PMID 8610120 DOI: 10.1073/Pnas.93.7.2795 |
0.602 |
|
| 1996 |
Zhang XL, Heng HH, Yang Y, Tsui LC, Parnes JR, Chamberlain JW. Chromosomal mapping of the second human CD8B gene locus. Immunogenetics. 43: 220-6. PMID 8575821 DOI: 10.1007/Bf00587303 |
0.602 |
|
| 1995 |
Marchese A, Heiber M, Nguyen T, Heng HH, Saldivia VR, Cheng R, Murphy PM, Tsui LC, Shi X, Gregor P. Cloning and chromosomal mapping of three novel genes, GPR9, GPR10, and GPR14, encoding receptors related to interleukin 8, neuropeptide Y, and somatostatin receptors. Genomics. 29: 335-44. PMID 8666380 DOI: 10.1006/Geno.1995.9996 |
0.555 |
|
| 1995 |
Heiber M, Docherty JM, Shah G, Nguyen T, Cheng R, Heng HH, Marchese A, Tsui LC, Shi X, George SR. Isolation of three novel human genes encoding G protein-coupled receptors. Dna and Cell Biology. 14: 25-35. PMID 7832990 DOI: 10.1089/Dna.1995.14.25 |
0.58 |
|
| 1995 |
Barron-Casella EA, Torres MA, Scherer SW, Heng HH, Tsui LC, Casella JF. Sequence analysis and chromosomal localization of human Cap Z. Conserved residues within the actin-binding domain may link Cap Z to gelsolin/severin and profilin protein families. The Journal of Biological Chemistry. 270: 21472-9. PMID 7665558 DOI: 10.1074/Jbc.270.37.21472 |
0.51 |
|
| 1995 |
Scherer SW, Heng HH, Robinson GW, Mahon KA, Evans JP, Tsui LC. Assignment of the human homolog of mouse Dlx3 to chromosome 17q21.3-q22 by analysis of somatic cell hybrids and fluorescence in situ hybridization. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 6: 310-1. PMID 7613049 DOI: 10.1007/Bf00352432 |
0.31 |
|
| 1995 |
O'Dowd BF, Scheideler MA, Nguyen T, Cheng R, Rasmussen JS, Marchese A, Zastawny R, Heng HH, Tsui LC, Shi X. The cloning and chromosomal mapping of two novel human opioid-somatostatin-like receptor genes, GPR7 and GPR8, expressed in discrete areas of the brain. Genomics. 28: 84-91. PMID 7590751 DOI: 10.1006/Geno.1995.1109 |
0.568 |
|
| 1994 |
Heng HH, Xiao H, Shi XM, Greenblatt J, Tsui LC. Genes encoding general initiation factors for RNA polymerase II transcription are dispersed in the human genome. Human Molecular Genetics. 3: 61-4. PMID 8162052 DOI: 10.1093/Hmg/3.1.61 |
0.307 |
|
| 1994 |
Wu J, Salido EC, Yen PH, Mohandas TK, Heng HH, Tsui LC, Park J, Chapman VM, Shapiro LJ. The murine Xe169 gene escapes X-inactivation like its human homologue. Nature Genetics. 7: 491-6. PMID 7951318 DOI: 10.1038/Ng0894-491 |
0.583 |
|
| 1994 |
Heng HH, Shi XM, Scherer SW, Andrulis IL, Tsui LC. Refined localization of the asparagine synthetase gene (ASNS) to chromosome 7, region q21.3, and characterization of the somatic cell hybrid line 4AF/106/KO15. Cytogenetics and Cell Genetics. 66: 135-8. PMID 7904551 DOI: 10.1159/000133685 |
0.349 |
|
| 1994 |
Heng HH, Tsui LC, Moens PB. Organization of heterologous DNA inserts on the mouse meiotic chromosome core. Chromosoma. 103: 401-7. PMID 7859560 DOI: 10.1007/Bf00362284 |
0.595 |
|
| 1994 |
Kunz J, Scherer SW, Klawitz I, Soder S, Du YZ, Speich N, Kalff-Suske M, Heng HH, Tsui LC, Grzeschik KH. Regional localization of 725 human chromosome 7-specific yeast artificial chromosome clones. Genomics. 22: 439-48. PMID 7806232 DOI: 10.1006/Geno.1994.1407 |
0.606 |
|
| 1994 |
Zhang XL, Lee KL, Heng HH, Tsui LC, Parnes JR, Shepherd NS, Chamberlain JW. Isolation of P1 bacteriophage clones containing large contiguous segments of the human and mouse loci for the T-cell coreceptor molecule CD8. Genetic Analysis, Techniques and Applications. 11: 129-39. PMID 7710778 DOI: 10.1016/1050-3862(94)90033-7 |
0.489 |
|
| 1993 |
Heng HH, Shi XM, Tsui LC. Fluorescence in situ hybridization mapping of the cystic fibrosis transmembrane conductance regulator (CFTR) gene to 7q31.3. Cytogenetics and Cell Genetics. 62: 108-9. PMID 8428507 DOI: 10.1159/000133451 |
0.307 |
|
| 1993 |
Heng HH, Tsui LC. Modes of DAPI banding and simultaneous in situ hybridization. Chromosoma. 102: 325-32. PMID 8325164 DOI: 10.1007/bf00661275 |
0.543 |
|
| 1993 |
Heng HH, Xie B, Shi XM, Tsui LC, Mahuran DJ. Refined mapping of the GM2 activator protein (GM2A) locus to 5q31.3-q33.1, distal to the spinal muscular atrophy locus. Genomics. 18: 429-31. PMID 8288250 DOI: 10.1006/Geno.1993.1491 |
0.597 |
|
| 1993 |
Marsden PA, Heng HH, Scherer SW, Stewart RJ, Hall AV, Shi XM, Tsui LC, Schappert KT. Structure and chromosomal localization of the human constitutive endothelial nitric oxide synthase gene. The Journal of Biological Chemistry. 268: 17478-88. PMID 7688726 |
0.344 |
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| 1992 |
Heng HH, Squire J, Tsui LC. High-resolution mapping of mammalian genes by in situ hybridization to free chromatin. Proceedings of the National Academy of Sciences of the United States of America. 89: 9509-13. PMID 1384055 DOI: 10.1073/Pnas.89.20.9509 |
0.606 |
|
| Show low-probability matches. |
